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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1090502Generated: November 2, 2026

Sodium Chloride → (2S,4R)-1-allyloxycarbonyl-2-carboxy-4-hydroxypyrrolidine

https://huagongshe.com/reaction/1090502

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantL-HydroxyprolineHCID 5810—
ReactantSodium HydroxideHCID 14798—
ReactantAllyl chloroformateHCID 18052—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2S,4R)-1-allyloxycarbonyl-2-carboxy-4-hydroxypyrrolidineHCID 18639171—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of (2S,4R)-2-carboxy-4-hydroxypyrrolidine (300 g) in a mixture of tetrahydrofuran (1.5 l) and water (1.5 l) was added dropwise a solution of allyl chloroformate (292 ml) in tetrahydrofuran (300 ml) at 0° C. while adjusting pH to around 9 with 4N aqueous sodium hydroxide. After stirring at 0° C. for 1 hour at pH 9, the aqueous layer was saturated with sodium chloride, and the mixture was diluted with ethyl acetate (1 l). The aqueous layer was separated, washed with ethyl acetate (1 l). After adjusting pH to around 2 with 12N hydrochloric acid, the emulsion was extracted with two portions of ethyl acetate (1 l×2). The combined extract was dried over magnesium sulfate and evaporated in vacuo to give (2S,4R)-1-allyloxycarbonyl-2-carboxy-4-hydroxypyrrolidine (426.2 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05081237
Source datasetuspto-grants-1992_01
ORD IDord-8c312ec966f64ca988fe4d62d487370a
Source noteuspto-grants-1992_01